Multi-stage polymer composition and films made therefrom

ABSTRACT

A multi-stage polymer composition comprising a crosslinked core having a Tg of from −85 to −10° C.; an intermediate region which comprises one or more intermediate layers, wherein each of the intermediate layers comprises from 88.5 to 99.9 weight percent of units derived from a one or more monomers selected from the group consisting of alkyl (meth)acrylate monomers, from 0 to 5 weight percent of units derived from a cross-linking monomer, a graft-linking monomer, or a combination of two or more thereof, optionally from 0 to 2 weight percent units derived from one or more chain transfer agents; wherein there is a compositional gradient between the intermediate layers such that the Tg transitions from −30° C. to 70° C. over the width of the intermediate region, and an outermost layer which has a Tg of from 40° C. to 110° C. is provided.

FIELD OF INVENTION

The instant invention relates to a multi-stage polymer composition andfilms made therefrom.

BACKGROUND OF THE INVENTION

A variety of indoor and outdoor products require flexible, transparent,and weather resistant plastic resins and films. Existing commercialresins comprising fluorine-containing polymers or aliphaticthermoplastic polyurethane (TPU) deliver the performance required bysuch indoor and outdoor products. However such resins are prohibitivelyexpensive for the majority of end uses. Low cost alternative resins areavailable, such as polyvinylchloride (PVC) resins containing plasticizerand polyethylene resins. However, such resins also present drawbacks,such as failure to meet all of the performance requirements and/orundesirable environmental impact.

Acrylic films made from existing resins manufactured via free radicalpolymerization process are generally too rigid for certain end useapplications, possess high moduli and poor tear resistance. Onecommercial acrylic resin currently available contains block copolymersof polymethylmethacrylate (PMMA) and polybutylacrylate (PBA) and isproduced by an anionic polymerization process. Such commercial resinspossess excellent flexibility and whitening resistance. However, themethod of producing this resin is very expensive, resulting in a resincost which is prohibitive for many applications.

SUMMARY OF THE INVENTION

The instant invention is a multi-stage polymer composition and filmsmade therefrom.

In one embodiment, the instant invention provides a multi-stage polymercomposition comprising: a crosslinked core which comprises greater than95 weight percent of units derived from one or more monomers selectedfrom the group consisting of alkyl (meth)acrylate monomers, from 0.1 to5 weight percent of units derived from a cross-linking monomer,graft-linking monomer, or combination thereof, and wherein thecrosslinked core has a Tg of from −85 to −10° C.; an intermediate regionwhich comprises one or more intermediate layers, wherein each of theintermediate layers comprises from 93 to 100 weight percent of unitsderived from a one or more monomers selected from the group consistingof alkyl (meth)acrylate monomers, from 0 to 5 weight percent of unitsderived from a cross-linking monomer, a graft-linking monomer, or acombination thereof, optionally from 0 to 2.0 weight percent unitsderived from one or more chain transfer agents; wherein there is acompositional gradient between the intermediate layers such that the Tgtransitions from −30° C. to 70° C. over the width of the intermediateregion, and an outermost layer which comprises from 98.5 to 100 weightpercent units derived from one or more monomers selected from the groupconsisting of alkyl (meth)acrylate, styrenic monomers, and combinations,from 0 to 1.5 weight percent units derived from one or more chaintransfer agents, and has a Tg of from 40° C. to 110° C.

BRIEF DESCRIPTION OF THE DRAWINGS

For the purpose of illustrating the invention, there is shown in thedrawings a form that is exemplary; it being understood, however, thatthis invention is not limited to the precise arrangements andinstrumentalities shown.

FIG. 1 is a graph of the heat capacity measured by DSC, for InventiveExample 1 and Comparative Example 1.

DETAILED DESCRIPTION OF THE INVENTION

The instant invention is a multi-stage polymer composition and filmsmade therefrom.

As used herein, the term “(meth)acrylate” means acrylate ormethacrylate.

The multi-stage polymer composition according to the present inventioncomprises: a crosslinked core which comprises greater than 95 to 99.9weight percent of units derived from one or more monomers selected fromthe group consisting of alkyl (meth)acrylate monomers, from 0.1 to 5weight percent of units derived from a cross-linking monomer,graft-linking monomer, or combination of two or more thereof, andwherein the crosslinked core has a Tg of from −85 to −10° C.; anintermediate region which comprises one or more intermediate layers,wherein each of the intermediate layers comprises up to 100 weightpercent of units derived from a one or more monomers selected from thegroup consisting of alkyl (meth)acrylate monomers, from 0 to 5 weightpercent of units derived from a cross-linking monomer, a graft-linkingmonomer, or a combination of two or more thereof, optionally from 0 to2.0 weight percent units derived from one or more chain transfer agents;wherein there is a compositional gradient between the intermediatelayers such that the Tg transitions from −30° C. to 70° C. over thewidth of the intermediate region, and an outermost layer which comprisesfrom 98.5 to 100 weight percent units derived from one or more monomersselected from the group consisting of alkyl (meth)acrylate, styrenicmonomers, and combinations of two or more thereof, from 0 to 1.5 weightpercent units derived from one or more chain transfer agents, and has aTg of from 40° C. to 110° C.

In an alternative embodiment, the instant invention further provides afilm comprising one or more embodiments of the multi-stage polymercomposition.

The crosslinked core comprises greater than 95 to 99.9 weight percent ofunits derived from one or more monomers selected from the groupconsisting of alkyl (meth)acrylate monomers. All individual values andsubranges from 95 to 99.9 weight percent are included herein anddisclosed herein; for example, the amount of units derived from one ormore alkyl (meth)acrylate monomers can be from a lower limit of 95,95.5, 96, 96.5, 97, 975, 98, 98.5, 99, or 99.5 weight percent to anupper limit of 95.3, 95.8, 96.3, 96.9, 97.5, 98, 98.7, 99.4 or 99.9weight percent. For example, the amount of units derived from one ormore alkyl (meth)acrylate monomers may be in the range of from 95 to99.9 weight percent, or in the alternative, the amount of units derivedfrom one or more alkyl (meth)acrylate monomers may be in the range offrom 95 to 97.5 weight percent, or in the alternative, amount of unitsderived from one or more alkyl (meth)acrylate monomers may be in therange of from 97.8 to 99.9 weight percent, or in the alternative, theamount of units derived from one or more alkyl (meth)acrylate monomersmay be in the range of from 96.5 to 97.9 weight percent.

The crosslinked core comprises from 0.1 to 5 weight percent of unitsderived from a cross-linking monomer, graft-linking monomer, orcombination thereof. All individual values and subranges from 0.1 to 5weight percent are included herein and disclosed herein; for example,the amount of units derived from cross-linking monomer, graft-linkingmonomer, or combination thereof can be from a lower limit of 0.1, 0.7,1.2, 1.9, 2.6, 3.1, 3.7, 4.4, or 4.9 weight percent, to an upper limitof 0.2, 0.8, 1.4, 2.1, 2.7, 3.3, 3.8, 4.5 or 5 weight percent. Forexample, the amount of units derived from cross-linking monomer,graft-linking monomer, or combination thereof may be in the range offrom 0.1 to 5 weight percent, or in the alternative, the amount of unitsderived from cross-linking monomer, graft-linking monomer, orcombination thereof may be in the range of from 0.5 to 2.5 weightpercent, or in the alternative, the amount of units derived fromcross-linking monomer, graft-linking monomer, or combination thereof maybe in the range of from 1.0 to 4.0 weight percent, or in thealternative, the amount of units derived from cross-linking monomer,graft-linking monomer, or combination thereof may be in the range offrom 0.3 to 3.5 weight percent.

The crosslinked core has a Tg of from −85 to −10° C. All individualvalues and subranges from −70 to −10° C. are included herein anddisclosed herein; for example, the Tg of the crosslinked core can befrom a lower limit of −85, −80 −70, −60, −50, −40, −30, −20, or −15° C.to an upper limit of −75, −65, −55, −45, −35, −25, −17 or −10° C. Forexample, the Tg of the crosslinked core may be in the range of from −85to −10° C., or in the alternative, the Tg of the crosslinked core may bein the range of from −60 to −40° C., or in the alternative, the Tg ofthe crosslinked core may be in the range of from −70 to −50° C., or inthe alternative, the Tg of the crosslinked core may be in the range offrom −50 to −30° C.

The intermediate region comprises one or more intermediate layers. Allindividual values and subranges from one or more intermediate layers isdisclosed herein and included herein. For example, the intermediateregion may comprise one, two, three, four, or five intermediate layers.

Each of the intermediate layers comprises up to 100 weight percent ofunits derived from a one or more monomers selected from the groupconsisting of alkyl (meth)acrylate monomers. All individual values andsubranges up to 100 weight percent are included herein and disclosedherein; for example, the amount of units derived from one or more alkyl(meth)acrylate monomers can be from a lower limit of 88.5, 89.4, 90.7,91.8, 92.6, 93.7, 94, 94.9, 95.5, 96, 97.4, 98.1, 99.3, 99.9 or 100weight percent. For example, the amount of units derived from one ormore alkyl (meth)acrylate monomers may be in the range of from 88.5 to100 weight percent, or in the alternative, the amount of units derivedfrom one or more alkyl (meth)acrylate monomers may be in the range offrom 90.5 to 99.9 weight percent, or in the alternative, the amount ofunits derived from one or more alkyl (meth)acrylate monomers may be inthe range of from 88.5 to 94.9 weight percent, or in the alternative,the amount of units derived from one or more alkyl (meth)acrylatemonomers may be in the range of from 92.5 to 96 weight percent.

Each of the intermediate layers comprises from 0 to 5 weight percent ofunits derived from a cross-linking monomer, a graft-linking monomer, ora combination of two or more thereof. All individual values andsubranges are disclosed herein and included herein; for example, theamount of units derived from a cross-linking monomer, a graft-linkingmonomer, or a combination thereof may be from a lower limit of 0, 0.5,1, 1.5, 2, 2.5, 3, 3.5, 4, or 4.5 weight percent to an upper limit of0.2, 0.7, 1.2, 1.7, 2.5, 2.7, 3.2, 3.7, 4.2, 4.7, or 5 weight percent.For example, the amount of units derived from a cross-linking monomer, agraft-linking monomer, or a combination of two or more thereof may be inthe range of from 0 to 5 weight percent, or in the alternative, theamount of units derived from a cross-linking monomer, a graft-linkingmonomer, or a combination of two or more thereof may be in the range offrom 0 to 2.5 weight percent, or in the alternative, the amount of unitsderived from a cross-linking monomer, a graft-linking monomer, or acombination of two or more thereof may be in the range of from 2.5 to 5weight percent, or in the alternative, the amount of units derived froma cross-linking monomer, a graft-linking monomer, or a combination oftwo or more thereof may be in the range of from 2 to 4 weight percent.

Each of the intermediate layers optionally comprises from 0 to 2.0weight percent units derived from one or more chain transfer agents. Allindividual values and subranges from 0 to 2.0 weight percent areincluded herein and disclosed herein; for example, the amount of unitsderived from one or more chain transfer agents can be from a lower limitof 0, 0.2, 0.4, 0.6, 0.8, 1.0, 1.2, 1.4, 1.6, 1.8 or 2.0 weight percentto an upper limit of 0.1, 0.3, 0.5, 0.7, 0.9, 1.1, 1.3, 1.7 or 1.9weight percent. For example, the amount of units derived from one ormore chain transfer agents may be in the range of from 0 to 2.0 weightpercent, or in the alternative, the amount of units derived from one ormore chain transfer agents may be in the range of from 0.75 to 2.0weight percent, or in the alternative, the amount of units derived fromone or more chain transfer agents may be in the range of from 0 to 0.75weight percent, or in the alternative, the amount of units derived fromone or more chain transfer agents may be in the range of from 0.5 to 1.0weight percent.

There is a compositional gradient between the intermediate layers suchthat the Tg transitions from −30° C. to 70° C. over the width of theintermediate region. All individual values and subranges from −30° C. to70° C. are included herein and disclosed herein; for example, the Tg cantransition from a lower limit of −30, −20, −10, 0, 10, 20, 30, 40, 50,or 60° C. to an upper limit of −25, −15, −5, 5, 15, 45, or 70° C. Forexample, the Tg can transition over the range of from −30 to 70° C., orin the alternative, the Tg can transition over the range of from −10 to30° C., or in the alternative, the Tg can transition over the range offrom −30 to −15° C., or in the alternative, or in the alternative, theTg can transition over the range of from −25 to 0° C., or in thealternative, the Tg can transition over the range of from 0 to 15° C.,or in the alternative, the Tg can transition over the range of from −15to 55° C., or in the alternative, the Tg can transition over the rangeof from 5 to 35° C.

Without being bound by any particular theory, it is believed that thecompositional gradient is achieved by the proper selection of and mannerand timing of addition of monomers during the emulsion polymerizationprocess used to prepare the intermediate region. Specifically, amulti-stage polymerization process is used during which monomers areadded in stages, rather than all at once, to the emulsion polymerizationreactor (or reactor vessel), permitting an interpenetration of one layerinto adjacent layers resulting in a Tg gradient over the intermediatestage. Such interpenetration as illustrated as per Inventive Example 1in FIG. 1.

The outermost layer comprises from 98.5 to 100 weight percent unitsderived from one or more monomers selected from the group consisting ofalkyl (meth)acrylate, styrenic monomers, and combinations of two or morethereof. All individual values and subranges from 98.5 to 100 weightpercent are included herein and disclosed herein; for example, theamount of units derived from one or more monomers selected from thegroup consisting of alkyl (meth)acrylate, styrenic monomers, andcombinations of two or more thereof can be from a lower limit of 98.5,98.7, 98.9, 99.1, 99.3, 99.5, 99.7, or 99.9 weight percent to an upperlimit of 98.6, 98.8, 99, 99.2, 99.4, 99.6, 99.8 or 100 weight percent.For example, the amount of units derived from one or more monomersselected from the group consisting of alkyl (meth)acrylate, styrenicmonomers, and combinations of two or more thereof may be in the range offrom 98.5 to 100 weight percent, or in the alternative, the amount ofunits derived from one or more monomers selected from the groupconsisting of alkyl (meth)acrylate, styrenic monomers, and combinationsof two or more thereof may be in the range of from 98.5 to 100 weightpercent, or in the alternative, the amount of units derived from one ormore monomers selected from the group consisting of alkyl(meth)acrylate, styrenic monomers, and combinations of two or morethereof may be in the range of from 98.5 to 100 weight percent, or inthe alternative, the amount of units derived from one or more monomersselected from the group consisting of alkyl (meth)acrylate, styrenicmonomers, and combinations of two or more thereof may be in the range offrom 98.5 to 100 weight percent, or in the alternative, the amount ofunits derived from one or more monomers selected from the groupconsisting of alkyl (meth)acrylate, styrenic monomers, and combinationsof two or more thereof may be in the range of from 98.5 to 99.6 weightpercent, or in the alternative, the amount of units derived from one ormore monomers selected from the group consisting of alkyl(meth)acrylate, styrenic monomers, and combinations of two or morethereof may be in the range of from 96.5 to 100 weight percent.

The outermost layer comprises from 0 to 1.5 weight percent units derivedfrom one or more chain transfer agents. All individual values andsubranges from 0 to 1.5 weight percent are included herein and disclosedherein; for example, the amount of units derived from one or more chaintransfer agents can be from a lower limit of 0, 0.2, 0.4, 0.6, 0.8, 1,1.2, or 1.4 weight percent to an upper limit of 0.1, 0.3, 0.5, 0.7, 0.9,1.1, 1.3, or 1.5 weight percent. For example, the amount of unitsderived from one or more chain transfer agents may be in the range offrom 0 to 1.5 weight percent, or in the alternative, the amount of unitsderived from one or more chain transfer agents may be in the range offrom 0 to 0.75 weight percent, or in the alternative, the amount ofunits derived from one or more chain transfer agents may be in the rangeof from 0.75 to 1.5 weight percent, or in the alternative, the amount ofunits derived from one or more chain transfer agents may be in the rangeof from 0.3 to 1.2 weight percent.

The outermost layer has a Tg of from 40° C. to 110° C. All individualvalues and subranges from 50° C. to 110° C. are included herein anddisclosed herein; for example, the Tg of the outermost layer can be froma lower limit of 40, 43, 45, 50, 60, 70, 80, 90, or 100° C. to an upperlimit of 55, 65, 75, 85, 95, 105, or 110° C. For example, the Tg of theoutermost layer may be in the range of from 40° C. to 110° C., or in thealternative, the Tg of the outermost layer may be in the range of from45° C. to 80° C., or in the alternative, the Tg of the outermost layermay be in the range of from 75° C. to 110° C., or in the alternative,the Tg of the outermost layer may be in the range of from 65° C. to 95°C.

“T_(g)” as used herein, is the glass transition temperature, of acopolymer calculated with the Fox equation [Bulletin of the AmericanPhysical Society 1, 3 Page 123 (1956)] as follows:

$\frac{1}{T_{g}} = {\frac{w_{1}}{T_{g{(1)}}} + \frac{w_{2}}{T_{g{(2)}}}}$

For a copolymer, w₁ and w₂ refer to the weight fraction of the twocomonomers, based on weight of monomers charged to the reaction vessel,and T_(g(1)) and T_(g(2)) refer to the glass transition temperatures ofthe two corresponding homopolymers in degrees Kelvin. For polymerscontaining three or more monomers, additional terms are added(w_(n)/T_(g(n)). The glass transition temperatures of homopolymers forthe purposes of this invention are those reported in “Polymer Handbook”,edited by J. Brandrup and E. H. Immergut, Interscience Publishers, 1966,unless that publication does not report the Tg of a particularhomopolymer, in which case the Tg of the homopolymer is measured bydifferential scanning colorimetry (DSC).

Weight average molecular weight (Mw) is determined by size exclusionchromatography using EasiCal PS-2® polystyrene standards supplied byPolymer Laboratories.

The alkyl (meth)acrylate monomers useful in the crosslinked core,intermediate layers, and outermost layer include linear and branchedalkyl (meth)acrylates wherein the alkyl group has from 1 to 12 carbonatoms. Exemplary useful alkyl groups include butyl acrylate, ethyl hexylacrylate, ethyl acrylate, methyl methacrylate, butyl methacrylate, andiso-octylacrylate.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the alkyl(meth)acrylate monomers of the crosslinked core are selected from thegroup consisting of butyl acrylate, ethyl hexyl acrylate, ethylacrylate, methyl methacrylate, and combinations of two or more thereof.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the alkyl(meth)acrylate monomers used in one or more intermediate layers areselected from the group consisting of butyl acrylate, ethyl hexylacrylate, ethyl acrylate, methyl methacrylate, cyclohexyl methacrylate,cyclopentyl acrylate, benzyl acrylate, benzyl methacrylate andcombinations of two or more thereof.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the alkyl(meth)acrylate of the outermost layer is selected from the groupconsisting of C1-C8 (meth)acrylates, and combinations of two or morethereof.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that styrenic monomers areused in the intermediate and/or outermost layers.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the styrenic monomersused in the outermost layer are selected from the group consisting ofstyrene, α-methylstyrene, vinyl toluene, and combinations of two or morethereof.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the styrenic monomersused in one or more intermediate layers are selected from the groupconsisting of styrene, α-methylstyrene, vinyl toluene, and combinationsof two or more thereof.

Cross-linking and/or graft-linking monomers useful in the crosslinkedcore and intermediate layers include, for example, butanedioldi(meth)acrylate, ethylene glycol di(meth)acrylate, divinyl benzene,diethylene glycol di(meth)acrylate, diallyl maleate, allyl methacrylate,diallyl phthalate, triallyl phthalate, trimethylolpropanetri(meth)acrylate, blends thereof and combinations of two or morethereof.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the cross-linkingmonomer of the crosslinked core is butanediol diacrylate.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the graft-linkingmonomer of the crosslinked core is allyl methacrylate.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the graft-linkingmonomer of the intermediate layer(s) is allyl methacrylate.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the crosslinked corecomprises greater than 95 weight percent units derived from acombination of butyl acrylate and butylene glycol diacrylate monomersand from 0.1 to 5 weight percent units derived from allyl methacrylatemonomer.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the one or moreintermediate layers each comprise units derived from butyl acrylate andmethyl methacrylate monomers.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the outermost layercomprises greater than 95 weight percent units derived from acombination of butyl acrylate and methyl methacrylate monomers.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition, in accordance with any of the precedingembodiments, except that the core component and adjacent intermediatelayer(s) component are formed by emulsion polymerization and form latexparticles having a size less than 250 nm.

“Particle size,” as used herein means weight average particle size ofthe emulsion (co)polymer particles as measured using a Brookhaven BI-90Particle Sizer. The particle size of the emulsion polymers used to formfilms of this invention may range from 30 to 250 nanometers. Allindividual values and subranges from 30 to 250 nm are disclosed hereinand included herein; for example, the average particle size may be froma lower limit of 30, 50, 70, 90, 110, 130, 150, 170, 190, 210, or 230 nmto an upper limit of 30, 60, 80, 100, 120, 140, 160, 180, 200, 220, 240or 250 nm. For example, the weight average particle size of the emulsion(co)polymer particles may range from 50 to 200 nanometers, or in thealternative, from 60 to 175, or in the alternative, from 90 to 175nanometers.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the weight averagemolecular weight (Mw) of the outermost layer composition is less than100,000 g/mole All individual values and subranges of less than 100,000g/mole are included herein and disclosed herein; for example, themolecular weight (Mw) of the outermost layer can be from an upper limitof 100,000; 80,000; 60,000; 40,000, 20,000; or 10,000 g/mole. Forexample, the molecular weight (Mw) of the outermost layer may be in therange of from 20,000 to 100,000 g/mole, or in the alternative, themolecular weight (Mw) of the outermost layer may be in the range of from40,000 to 80,000 g/mole, or in the alternative, the molecular weight(Mw) of the outermost layer may be in the range of from 40,000 to 60,000g/mole, or in the alternative, the molecular weight (Mw) of theoutermost layer may be in the range of from 40,000 to 50,000 g/mole, orin the alternative, the molecular weight (Mw) of the outermost layer maybe in the range of from 20,000 to 30,000 g/mole.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the film exhibits oneor more of the following properties: a modulus of 30,000 psi or less;and an elongation at break of at least 200%. All individual values andsubranges from a modulus of 30,000 psi or less are included herein anddisclosed herein; for example, the modulus can be from an upper limit of30,000; 25,000, 20,000; 19,000; 18,000; or 17,000 psi. For example, thefilm modulus may be in the range of from 18,000 to 30,000 psi, or in thealternative, the film modulus may be in the range of from 25,000 to30,000 psi, or in the alternative, the film modulus may be in the rangeof from 19,500 to 20,000 psi. All individual values and subranges from aelongation at break of at least 200% are included herein and disclosedherein; for example, the elongation at break can be from a lower limitof 200%, 190%, 180%, or 170%. In one embodiment the elongation at breakof the film has a lower limit of 150%.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the film having athickness of 300 μm or less exhibits one or more of the followingproperties: a haze of less than 1.5%; a yellowness index of less than1%. All individual values and subranges of a haze of less than 1% areincluded herein and disclosed herein; for example, the haze can be froman upper limit of 1%, 0.9%, or 0.8%. In one embodiment, the haze of thefilm has a lower limit of 0.5%. All individual values and subranges of ayellowness index of less than 1% are included herein and disclosedherein; for example, the yellowness index can be from an upper limit of1%, 0.9%, or 0.8%. In one embodiment, the yellowness index of the filmhas a lower limit of 0.5%.

In an alternative embodiment of the invention, the multi-stage polymercomposition according to any one of the foregoing embodiments may beformed into sheets. End use applications for such sheets include, butare not limited to, glass laminates and interlayers for use inautomotive windows and windshields, and for use in hurricane resistantglass windows and/or doors. Sheets made from the inventive polymercompositions may have any appropriate thickness. In one embodiment, thesheet is between 150 and 500 microns.

In an alternative embodiment, the instant invention provides amulti-stage polymer composition and films made therefrom, in accordancewith any of the preceding embodiments, except that the film furthercomprises one or more additives selected from the group consisting ofstabilizers, and plasticizers.

Multi-stage polymer composition and films made therefrom can alsocontain other ingredients that include, but are not limited to, dyes,pigments, flameproofing agents, internal and external lubricants, slipaids, impact modifiers, processing aids, blowing agents, fillers andwith other additives to prevent, reduce or mask discoloration ordeterioration caused by heating, aging, exposure to light or weathering.

The multi-stage polymer composition can be processed into film and/orsheet by way of extrusion, calendaring, or injection molding.

In yet another embodiment, the invention provides a multi-stage polymercomposition consisting essentially of: a crosslinked core whichcomprises greater than 95 weight percent of units derived from one ormore monomers selected from the group consisting of alkyl (meth)acrylatemonomers, from 0.1 to 5 weight percent of units derived from across-linking monomer, graft-linking monomer, or combination thereof,and wherein the crosslinked core has a Tg of from −85 to −10° C.; anintermediate region which comprises one or more intermediate layers,wherein each of the intermediate layers comprises from 88.5 to 100weight percent of units derived from a one or more monomers selectedfrom the group consisting of alkyl (meth)acrylate monomers, from 0 to 5weight percent of units derived from a cross-linking monomer, agraft-linking monomer, or a combination of two or more thereof,optionally from 0 to 2.0 weight percent units derived from one or morechain transfer agents; wherein there is a compositional gradient betweenthe intermediate layers such that the Tg transitions from −30° C. to 70°C. over the width of the intermediate region, and an outermost layerwhich comprises from 98.5 to 100 weight percent units derived from oneor more monomers selected from the group consisting of alkyl(meth)acrylate, styrenic monomers, and combinations of two or morethereof, from 0 to 1.5 weight percent units derived from one or morechain transfer agents, and has a Tg of from 40° C. to 110° C.

In yet another embodiment, the invention provides a multi-stage polymercomposition comprising: a crosslinked core which consists essentially ofgreater than 95 weight percent of units derived from one or moremonomers selected from the group consisting of alkyl (meth)acrylatemonomers, from 0.1 to 5 weight percent of units derived from across-linking monomer, graft-linking monomer, or combination thereof,and wherein the crosslinked core has a Tg of from −85 to −10° C.; anintermediate region which comprises one or more intermediate layers,wherein each of the intermediate layers comprises from 88.5 to 100weight percent of units derived from a one or more monomers selectedfrom the group consisting of alkyl (meth)acrylate monomers, from 0 to 5weight percent of units derived from a cross-linking monomer, agraft-linking monomer, or a combination of two or more thereof,optionally from 0 to 2.0 weight percent units derived from one or morechain transfer agents; wherein there is a compositional gradient betweenthe intermediate layers such that the Tg transitions from −30° C. to 70°C. over the width of the intermediate region, and an outermost layerwhich comprises from 98.5 to 100 weight percent units derived from oneor more monomers selected from the group consisting of alkyl(meth)acrylate, styrenic monomers, and combinations of two or morethereof, from 0 to 1.5 weight percent units derived from one or morechain transfer agents, and has a Tg of from 40° C. to 110° C.

In yet another embodiment, the invention provides a multi-stage polymercomposition comprising: a crosslinked core which comprises greater than95 weight percent of units derived from one or more monomers selectedfrom the group consisting of alkyl (meth)acrylate monomers, from 0.1 to5 weight percent of units derived from a cross-linking monomer,graft-linking monomer, or combination thereof, and wherein thecrosslinked core has a Tg of from −85 to −10° C.; an intermediate regionwhich comprises one or more intermediate layers, wherein each of theintermediate layers consists essentially of from 88.5 to 100 weightpercent of units derived from a one or more monomers selected from thegroup consisting of alkyl (meth)acrylate monomers, from 0 to 5 weightpercent of units derived from a cross-linking monomer, a graft-linkingmonomer, or a combination of two or more thereof, optionally from 0 to2.0 weight percent units derived from one or more chain transfer agents;wherein there is a compositional gradient between the intermediatelayers such that the Tg transitions from −30° C. to 70° C. over thewidth of the intermediate region, and an outermost layer which comprisesfrom 98.5 to 100 weight percent units derived from one or more monomersselected from the group consisting of alkyl (meth)acrylate, styrenicmonomers, and combinations of two or more thereof, from 0 to 1.5 weightpercent units derived from one or more chain transfer agents, and has aTg of from 40° C. to 110° C.

In yet another embodiment, the invention provides a multi-stage polymercomposition comprising: a crosslinked core which comprises greater than95 weight percent of units derived from one or more monomers selectedfrom the group consisting of alkyl (meth)acrylate monomers, from 0.1 to5 weight percent of units derived from a cross-linking monomer,graft-linking monomer, or combination thereof, and wherein thecrosslinked core has a Tg of from −85 to −10° C.; an intermediate regionwhich comprises one or more intermediate layers, wherein each of theintermediate layers comprises from 88.5 to 100 weight percent of unitsderived from a one or more monomers selected from the group consistingof alkyl (meth)acrylate monomers, from 0 to 5 weight percent of unitsderived from a cross-linking monomer, a graft-linking monomer, or acombination of two or more thereof, optionally from 0 to 2.0 weightpercent units derived from one or more chain transfer agents; whereinthere is a compositional gradient between the intermediate layers suchthat the Tg transitions from −30° C. to 70° C. over the width of theintermediate region, and an outermost layer which consists essentiallyof from 98.5 to 100 weight percent units derived from one or moremonomers selected from the group consisting of alkyl (meth)acrylate,styrenic monomers, and combinations of two or more thereof, from 0 to1.5 weight percent units derived from one or more chain transfer agents,and has a Tg of from 40° C. to 110° C.

In yet an alternative embodiment, the invention provides a sheet or filmconsisting essentially of one or more of the multi-stage polymercomposition according to any of the foregoing embodiments.

EXAMPLES

The following examples illustrate the present invention but are notintended to limit the scope of the invention.

Inventive Example 1

The components used in preparing Inventive Example 1 are shown in Table1.

A reactor equipped with a stirrer and condenser and blanked withnitrogen was charged with Mixture A. Into the stirred reactor at 85° C.were added Mixture B, 7% of Mixture C, 1.7% of Mixture D and 10.4% ofMixture E. After an exothermic reaction took place and the reactorreached peak temperature, the heating and stirring were continued at 85°C. for 5 minutes. The remainder of Mixture C and 8.7% of Mixture D weregradually added to the reactor over 90 minutes. After the addition wascomplete, the reactor was kept at 85° C. for 15 minutes. 24.3% ofMixture E was added to the reactor. Mixture F and 24.3% of Mixture Dwere gradually added to the reactor over 90 minutes. After the additionwas complete, the reactor was held at 85° C. for 15 minutes. 21.9% ofMixture E was added to the reactor. Mixture G and 21.9% of Mixture Dwere gradually added to the reactor over 60 minutes. After the additionwas complete, the reactor was held at 85° C. for 15 minutes. Theremainder of Mixture E was added to the reactor. Mixture H and theremainder of Mixture D were gradually added to the reactor over 60minutes. After the addition was complete, the reactor was held at 85° C.for 15 minutes, then cooled to ambient temperature.

TABLE 1 Parts Mixture Component by Weight A Water 385 23% Aqueous sodiumdodecylbenzenesulfonate 2.5 B 0.2% Aqueous iron sulfate heptahydrate1.21 0.5% Aqueous ethylenediaminetetracetic acid 1.02 Water 5 C Butylacrylate 124.4 1,3-Butanediol diacrylate 1.26 Allyl methacrylate 0.6323% Aqueous sodium dodecylbenzenesulfonate 3.9 Water 35 D 70% aqueoustert-butylhydroperoxide 0.38 Water 14.8 E Sodium hydroxymethanesulfinatehydrate 0.47 Water 23.8 F Butyl acrylate 80.9 Methyl methacrylate 43.6Allyl methacrylate 0.63 23% Aqueous sodium dodecylbenzenesulfonate 3.8Water 35 G Butyl acrylate 13.7 Methyl methacrylate 39.6 1-dodecanethiol0.22 23% Aqueous sodium dodecylbenzenesulfonate 2.3 Water 13.5 H Butylacrylate 13.7 Methyl methacrylate 39.6 1-dodecanethiol 0.92 23% Aqueoussodium dodecylbenzenesulfonate 2.3 Water 13.5Inventive Example 1 had an average particle size of 164 nm, a solidscontent of 39.3%, and a weight average molecular weight of 42,400 g/mol.

Comparative Example 1

Table 2 shows the components used in preparing Comparative Example 1.Comparative Example 1 is prepared by a 4-stage acrylic aqueous emulsionpolymerization:

A reactor equipped with a stirrer and condenser and blanked withnitrogen was charged with Mixture A. Into the stirred reactor at 83° C.were added 7% of Mixture B, 1.8% of Mixture D and 11.3% of Mixture E.After an exothermic reaction took place and the reactor reached peaktemperature, the heating and stirring were continued at 85° C. for 5minutes. The remainder of Mixture B, Mixture C and 8.7% of Mixture Dwere gradually added to the reactor over 90 minutes. After the additionwas complete, the reactor was kept at 85° C. for 15 minutes. 38.9% ofMixture E was added to the reactor. Mixture F and 9.4% of Mixture D weregradually added to the reactor over 90 minutes. After the addition wascomplete, the reactor was held at 85° C. for 15 minutes. 16.8% ofMixture E was added to the reactor. Mixture G and 21.5% of Mixture Dwere gradually added to the reactor over 60 minutes. After the additionwas complete, the reactor was held at 85° C. for 15 minutes. Theremainder of Mixture E was added to the reactor. Mixture H and theremainder of Mixture D were gradually added to the reactor over 60minutes. After the addition was complete, the reactor was held at 85° C.for 15 minutes, then cooled to ambient temperature.

TABLE 2 Parts Mixture Component by Weight A Deionized Water 387.5 23%Aqueous sodium dodecylbenzenesulfonate 2.6 B Butyl acrylate 124.41,3-Butanediol diacrylate 1.26 Allyl methacrylate 0.63 23% Aqueoussodium dodecylbenzenesulfonate 2.9 Water 35 C 23% Aqueous sodiumdodecylbenzenesulfonate 2.82 Water 3.75 D 70% aqueoustert-butylhydroperoxide 0.35 Water 12.3 E Sodium hydroxymethanesulfinatehydrate 0.43 Water 16.3 F Butyl acrylate 49.8 Methyl methacrylate 74.7Allyl methacrylate 0.63 23% Aqueous sodium dodecylbenzenesulfonate 5.45Water 35 G Butyl acrylate 13.7 Methyl methacrylate 39.6 1-dodecanethiol0.22 23% Aqueous sodium dodecylbenzenesulfonate 2.3 Water 13.5 H Butylacrylate 13.7 Methyl methacrylate 39.6 1-dodecanethiol 0.92 23% Aqueoussodium dodecylbenzenesulfonate 2.3 Water 13.5Comparative Example 1 had a particle size of 219 nm, a solids content of38.9% and a weight average molecular weight of 29,300 g/mole.

As can be seen in FIG. 1, Inventive Example 1 exhibits less distinctheat capacity peaks for the intermediate stage of the polymercomposition, indicating a compositional gradient, rather than distinctintermediate layers.

The emulsion prepared from each of Inventive Example 1 and ComparativeExample 1 above was freeze dried with a vacuum oven, and the resultantpowder was then processed using a Collin Mill (W. H. Collin GmbHMaschienefabrik, Aichach, Germany) at 160° C. for 3 minutes. After themilling was completed, the molten polymer was peeled from the metalrolls and cooled down to provide film with a thickness in the range from190 to 250 μm.

TABLE 3 Film thickness Elongation@break stress@ yield stress@breakModulus Stress Units (microns) (%) (psi) (psi) (psi) whiteningComparative 205 297 2650 2910 46200 Yes Example 1 Inventive 190 321 6791628 12160 No Example 1

TABLE 4 Haze Y Total (%) (%) L a b YI Comparative 2.67 92.6 96.7 −0.3841.428 2.35 Example 1 Inventive 0.89 93.3 97.0 −0.066 0.508 0.89 Example1

Test Methods GPC Molecular Weight

The term “molecular weight” as used herein refers to peak averagemolecular weight as determined by gel permeation chromatography (GPC)against narrow molecular weight polystyrene standards in tetrahydrofuransolvent at 25° C. using Polymer Laboratories data manipulation software.

Particle Size

The volume average particle size was measured on very dilute latexes(diluted to 0.001% solids) with a BI 90 (Brookhaven Instruments,Holtsville, N.Y.) particle size detector, utilizing Dynamic LightScattering (15° and 90° scattering angles) and a laser light source. Thesignal is detected by a photodiode array and the data analyzed with abuilt in correlator.

Differential Scanning Calorimetry (DSC)

The glass transition temperature (Tg) was measured using a differentialscanning calorimetry (DSC) from TA Instruments (New Castle, Del., USA).Samples were tested in an aluminum pan under N₂ under a rate of 20°C./min.

Haze Level

Haze level of films was measured in accordance with ASTM 871-96 (2010).

Film Thickness

The thickness of the films was measured using a micrometer.

Optical Properties

Optical properties were measured using a Color Quest II, from HunterLabs. (Reston, Va., USA).

The present invention may be embodied in other forms without departingfrom the spirit and the essential attributes thereof, and, accordingly,reference should be made to the appended claims, rather than to theforegoing specification, as indicating the scope of the invention.

1. A multi-stage polymer composition comprising: a crosslinked corewhich comprises greater than 95 weight percent of units derived from oneor more monomers selected from the group consisting of alkyl(meth)acrylate monomers, from 0.1 to 5 weight percent of units derivedfrom a cross-linking monomer, graft-linking monomer, or combinationthereof, and wherein the crosslinked core has a Tg of from −85 to −10°C.; an intermediate region which comprises one or more intermediatelayers, wherein each of the intermediate layers comprises from 88.5 to100 weight percent of units derived from a one or more monomers selectedfrom the group consisting of alkyl (meth)acrylate monomers, from 0 to 5weight percent of units derived from a cross-linking monomer, agraft-linking monomer, or a combination of two or more thereof,optionally from 0 to 2.0 weight percent units derived from one or morechain transfer agents; wherein there is a compositional gradient betweenthe intermediate layers such that the compositional gradient transitionsbetween a lower Tg and an upper Tg, wherein said lower Tg is at least−10° C. and said upper Tg is 70° C. or less over the width of theintermediate region, and an outermost layer which comprises from 98.5 to100 weight percent units derived from one or more monomers selected fromthe group consisting of alkyl (meth)acrylate, styrenic monomers, andcombinations of two or more thereof, from 0 to 1.5 weight percent unitsderived from one or more chain transfer agents, and has a Tg of from 40°C. to 110° C.
 2. The multi-stage polymer composition according to claim1, wherein the outermost layer has a Tg of from 50° C. to 97° C.
 3. Themulti-stage polymer composition according to claim 1, wherein thecrosslinked core has a Tg of from −55 to −30 C.
 4. The multi-stagepolymer composition according to claim 1, wherein the cross-linkingmonomer of the crosslinked core, the graft-linking monomer of thecrosslinked core, the cross-linking monomer of the intermediate layer(s)and the graft-linking monomer of the intermediate layer(s) are selectedfrom the group consisting of butanediol di(meth)acrylate, ethyleneglycol di(meth)acrylate, divinyl benzene, diethylene glycoldi(meth)acrylate, trimethylolpropane triacrylate, butylene glycoldimethacrylate, blends thereof, and combinations of two or more thereof.5. The multi-stage polymer composition according to claim 1, wherein thecross-linking monomer of the crosslinked core and the cross-linkingmonomer of the intermediate layer(s) are selected from the groupconsisting allyl methacrylate, diallyl maleate, blends thereof, andcombinations of two or more thereof.
 6. The multi-stage polymercomposition according to claim 1, wherein the cross-linking monomer ofthe crosslinked core is butanediol diacrylate, the graft-linking monomerof the crosslinked core is allyl methacrylate and the graft-linkingmonomer of the intermediate layer(s) is allyl methacrylate.
 7. Themulti-stage polymer composition according to claim 1, wherein the alkyl(meth)acrylate monomers of the crosslinked core are selected from thegroup consisting of butyl acrylate, ethyl hexyl acrylate, ethylacrylate, methyl methacrylate, and combinations of two or more thereof.8. The multi-stage polymer composition according to claim 1, wherein thealkyl (meth)acrylate monomers of the intermediate layer(s) are selectedfrom the group consisting of butyl acrylate, ethyl hexyl acrylate, ethylacrylate, methyl methacrylate, cyclohexyl (meth)acrylate, cyclopentylmethacrylate, tetrahydrofurfyl methacrylate, benzyl (meth)acryale andcombinations of two or more thereof.
 9. The multi-stage polymercomposition according to claim 1, wherein the alkyl (meth)acrylatemonomers of the outermost layer are selected from the group consistingof butyl acrylate, ethyl hexyl acrylate, ethyl acrylate, methylmethacrylate, and combinations of two or more thereof.
 10. Themulti-stage polymer composition according to claim 1, wherein thecrosslinked core comprises at least 95 weight percent units of butylacrylate and from 0.1 to 5.0 weight percent units of a combination ofbutylene glycol diacrylate and allyl methacrylate. 95 weight percentunits derived from a combination of butyl acrylate and butylene glycoldiacrylate monomers and from 0.1 to 5 weight percent units derived fromallyl methacrylate.
 11. The multi-stage polymer composition according toclaim 1, wherein the one or more intermediate layers each comprise unitsderived from butyl acrylate and methyl methacrylate.
 12. The multi-stagepolymer composition according to claim 1, wherein the outermost layercomprises greater than 95 weight percent units derived from acombination of butyl acrylate and methyl methacrylate monomers.
 13. Themulti-stage polymer composition according to claim 1 are formed byemulsion polymerization, wherein the latex particles having an averageparticle size less than 250 nm.
 14. The multi-stage polymer compositionaccording to claim 1, wherein the weight average (M_(w)) molecularweight of the outermost layer composition is less than 50,000 g/mol. 15.A film or sheet comprising the multi-stage polymer composition accordingto claim
 1. 16. The film or sheet according to claim 15, wherein thefilm exhibits one or more of the following properties: a modulus of30,000 psi or less; and an elongation at break of at least 200%.
 17. Thefilm or sheet according to claim 15, wherein the film or sheet has athickness of from 3 mil to 12 mil and exhibits one or more of thefollowing properties: a haze of less than 1%; and a yellowness index ofless than 1%.